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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392091Generated: October 30, 2026

4-Methylmorpholine → HCID 10435474, compound

https://huagongshe.com/reaction/1392091

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(2S)-2-[[2-(3,5-difluorophenyl)acetyl]amino]propanoic acidHCID 12135350—
ReactantHCID 58691198HCID 58691198—
SolventDichloromethaneHCID 6344—
ProductHCID 10435474HCID 1043547480.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (3S,7S)-3-amino-1-(2-methoxyethyl)-7-phenyl-1,3,4,7-tetrahydro-2H-azepin-2-one (6d) (55 mg) in DCM (4 mL) at 0° C. under N2 was added N-[(3,5-difluorophenyl)acetyl]-L-alanine (51 mg), HOBt-hydrate (71 mg), EDAC.HCl (61 mg) and N-methyl morpholine (34 mg). The reaction mixture was stirred 1 h at 0° C. and 3 h at RT, then diluted with 30% hexanes/EtOAc (100 mL). The organic phase was consecutively washed with H2O, 0.2 N HCl, saturated NaHCO3, and brine, dried (Na2SO4), filtered and evaporated. The crude product was purified by flash chromatography (1%-2% MeOH/DCM) to afford a white solid (82 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342007B2
Source datasetuspto-grants-2008_03
ORD IDord-5bbf42c416644fbba99fe8ac96959a53
Source noteuspto-grants-2008_03